Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts

Phytochemical analysis of the methanolic and dichloromethane extracts of the aerial parts of Scutellaria pinnatifida led to the isolation of a phenylpropanoid, 1-o-feruloyl-ß-D-glucose [1], two known flavonoids including luteolin-7-o-glucoside (2) and apigenin-7-o-glucoside (3), three known phenylet...

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Main Authors: Abbas Delazar, Hossein Nazemiyeh, Fariba Heshmati Afshar, Niloofar Barghi, Solmaz Esnaashari, Parina Asgharian
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Research in Pharmaceutical Sciences
Subjects:
Online Access:http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2017;volume=12;issue=3;spage=187;epage=195;aulast=Delazar
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spelling doaj-a2c8399a5ee54a3c91e5df11e3d5a6892021-07-07T14:25:35ZengWolters Kluwer Medknow PublicationsResearch in Pharmaceutical Sciences1735-53621735-94142017-01-0112318719510.4103/1735-5362.207199Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial partsAbbas DelazarHossein NazemiyehFariba Heshmati AfsharNiloofar BarghiSolmaz EsnaashariParina AsgharianPhytochemical analysis of the methanolic and dichloromethane extracts of the aerial parts of Scutellaria pinnatifida led to the isolation of a phenylpropanoid, 1-o-feruloyl-ß-D-glucose [1], two known flavonoids including luteolin-7-o-glucoside (2) and apigenin-7-o-glucoside (3), three known phenylethanoid glycosides composed of phlomisethanoside (4), syringalide A (5), and verbascoside (6), and oleic acid (7). Isolation and structural elucidation of compounds were accomplished by HPLC and spectroscopic methods (UV, 1H- NMR, 13C-NMR). The extracts were also evaluated for their radical scavenging activity and insecticidal property by 2,2-diphenyl-1-picryl-hydrazyl (DPPH) assay and contact toxicity method, respectively. Among the extracts, the methanol extract showed the most potent free radical scavenging activity with a RC50 value of 0.044 ± 0.350 mg/mL which could be attributed to the presence of the isolated phenolic compounds. In the case of insecticidal activity, the n-hexane extract displayed the most potent activity and caused 10%, 15%, and 40% mortality to Oryzaephilus mercator at the concentration of 5, 10, and 15 mg/mL after 4 h of exposure.http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2017;volume=12;issue=3;spage=187;epage=195;aulast=Delazarscutellaria pinnatifida; phenylpropanoid; antioxidant activity; insecticidal activity
collection DOAJ
language English
format Article
sources DOAJ
author Abbas Delazar
Hossein Nazemiyeh
Fariba Heshmati Afshar
Niloofar Barghi
Solmaz Esnaashari
Parina Asgharian
spellingShingle Abbas Delazar
Hossein Nazemiyeh
Fariba Heshmati Afshar
Niloofar Barghi
Solmaz Esnaashari
Parina Asgharian
Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts
Research in Pharmaceutical Sciences
scutellaria pinnatifida; phenylpropanoid; antioxidant activity; insecticidal activity
author_facet Abbas Delazar
Hossein Nazemiyeh
Fariba Heshmati Afshar
Niloofar Barghi
Solmaz Esnaashari
Parina Asgharian
author_sort Abbas Delazar
title Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts
title_short Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts
title_full Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts
title_fullStr Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts
title_full_unstemmed Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts
title_sort chemical compositions and biological activities of scutellaria pinnatifida a. hamilt aerial parts
publisher Wolters Kluwer Medknow Publications
series Research in Pharmaceutical Sciences
issn 1735-5362
1735-9414
publishDate 2017-01-01
description Phytochemical analysis of the methanolic and dichloromethane extracts of the aerial parts of Scutellaria pinnatifida led to the isolation of a phenylpropanoid, 1-o-feruloyl-ß-D-glucose [1], two known flavonoids including luteolin-7-o-glucoside (2) and apigenin-7-o-glucoside (3), three known phenylethanoid glycosides composed of phlomisethanoside (4), syringalide A (5), and verbascoside (6), and oleic acid (7). Isolation and structural elucidation of compounds were accomplished by HPLC and spectroscopic methods (UV, 1H- NMR, 13C-NMR). The extracts were also evaluated for their radical scavenging activity and insecticidal property by 2,2-diphenyl-1-picryl-hydrazyl (DPPH) assay and contact toxicity method, respectively. Among the extracts, the methanol extract showed the most potent free radical scavenging activity with a RC50 value of 0.044 ± 0.350 mg/mL which could be attributed to the presence of the isolated phenolic compounds. In the case of insecticidal activity, the n-hexane extract displayed the most potent activity and caused 10%, 15%, and 40% mortality to Oryzaephilus mercator at the concentration of 5, 10, and 15 mg/mL after 4 h of exposure.
topic scutellaria pinnatifida; phenylpropanoid; antioxidant activity; insecticidal activity
url http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2017;volume=12;issue=3;spage=187;epage=195;aulast=Delazar
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